Apparatus for injection analysis of total inorganic phosphate

ABSTRACT

A method for flow injection analysis of total inorganic phosphate contained in an aqueous system such as a cooling tower or boiler is described which uses a reducing agent and preservative composition therefore as the carrier for the sample to be analyzed, thereby creating a facile process which permits conversion of the various polyphosphates to orthophosphate and development of the molybdenum blue complex color reaction at 60°-95° C. and under 2-10 psi. This method has less stringent pressure and temperature requirements than those employed heretofore, thus permitting the use of more reliable and economic devices for measuring total inorganic phosphate in the field.

REFERENCE TO RELATED APPLICATIONS

This is a continuation-in-part of application Ser. No. 07/745,638C-1521IA, filed Aug. 15, 1991, which is a continuation-in-part ofapplication Ser. No. 597,650, filed Oct. 15, 1990, now abandoned.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention is in the field of methods and apparatus for flowinjection analysis of total inorganic phosphate in aqueous systems.Inorganic phosphates such as orthophosphate and polyphosphate areproducts which are used in aqueous systems such as cooling towers andboilers to prevent calcium scales and corrosion. There is a thresholdconcentration at which phosphates work by causing crystal distortionthat prevents calcium scale and/or steel corrosion. Thus, it isimportant to determine on a regular basis the concentration of dissolvedinorganic phosphates so that the threshold levels necessary to preventdeposition of calcium scales is maintained. A secondary goal is toprevent high phosphate concentrations which may result in subsequentphosphate scale.

However, the analytical measurement of these inorganic phosphates isimportant in other fields such as environmental, clinical andagricultural analysis, where the determination of inorganic phosphatelevels can also be important, as, for example, the determination of thephosphate levels in fertilizers or in clinical specimens such as plasma.The novel method of the present invention is applicable to these areasas well.

Flow injection analysis (FIA) is a well-known, simple and reliabletechnique based on continuous flow of a sample solution which isintroduced directly into an unsegmented carrier stream of a reagentsolution, thereby forming a well-defined sample zone. In so calledreverse flow injection analysis, the reagent is introduced into anunsegmented sample stream. While it is being transported to a detectordevice further downstream, the sample has an opportunity to react withthe reagent and form a new chemical species which can be quantitativelymeasured by the detector. The reaction is usually a color-forming oneand the detector, therefore, a colorimeter (spectrophotometer). FIAlends itself to the automated, rapid and reliable analysis of varioussamples, and offers many advantages over the older technique ofair-segmented continuous flow analysis.

Apparatus means for carrying out a typical FIA method will depend uponthe reaction being carried out, but elements which are almost alwayspresent include tubing through which the samples and reagents arecarried, means for moving said samples and reagents through said tubingand means for mixing them together, reagent reservoirs, means forcollecting, filtering and supplying samples, heating, and analyzer meanssuch as a colorimeter.

The color-forming reaction which has been used in the past to provide ameans for quantitatively analyzing inorganic phosphate content is thewell-established one wherein a mixed solution of molybdenum (V) andmolybdenum (VI) reacts with orthophosphate to produce the heteropolyblue complex. It is well known that orthophosphate (P₁) reacts with amolybdenum (VI) reagent to form a yellow heteropoly complex and thatsubsequent reduction of the yellow complex by ascorbic acid or othersuitable reductants gives heteropoly blue complex containing Mo(V) andMo(VI). The formation of these heteropoly complexes has been extensivelyapplied to the determination of phosphorus by flow injection analysisand by air-segmented flow analysis.

The total inorganic phosphate content of a sample to be analyzed willusually never be all orthophosphate; however, so that the color-formingreaction described above cannot be utilized. It is necessary to firstconvert the various types of inorganic phosphates present toorthophosphate in order to proceed with the flow injection analysis.Typically, the inorganic phosphates which are not orthophosphates arepolyphosphates, which have the general formula M_(x+2) P_(x) O_(3x+1),and include, e.g., pyrophosphate (diphosphate, P₂) and tripolyphosphate(triphosphate, P₃). These polyphosphates may be converted toorthophosphate by hydrolysis using concentrated sulfuric acid or otherinorganic acids at high temperatures (>100° C.) and pressures for asuitable period of time, in accordance with well known proceduresemployed in FIA.

Typically, the acid hydrolysis reagent, e.g., concentrated sulfuricacid, is combined with the color-forming reagent, i.e., the Mo (V andVI), by dissolving the latter in the former. After the inorganicphosphates are converted to orthophosphate with this combined reagent athigh temperature and pressure, and the yellow heteropoly complex isformed, in a subsequent step ascorbic acid or other reducing agent isadded to the reaction mixture to form the heteropoly blue complex, whichis then measured on a colorimeter.

Of course, it is also possible to use the method of the presentinvention to provide for the flow injection analysis of orthophosphateonly, if that is desired. This may be accomplished using the same methodas for polyphosphate, except that during the step of heating thereaction mixture to convert polyphosphate to orthophosphate, thereaction temperature is maintained at a lower level, sufficient for thecolor-forming reaction to proceed.

2. Brief Description of the Prior Art

Elemental analysis of inorganic phosphates using methods and devicesother than flow injection analysis are well known; see, e.g. U.S. Pat.Nos. 3,137,543; 3,846,074; and 4,836,773.

Hirai et al., Anal. Chim. Acta, 115, 269-277 (1980), describe a flowinjection analysis method for inorganic polyphosphates, but employ hightemperatures (140° C.) and pressures (5 kg cm⁻² =@ 70 psi). A solutionof 0.1M L-ascorbic acid containing 50 mL of acetone is employed, butthis is in a segmented flow analysis method and is used as a reducingagent for the molybdenum reagent in the color-forming step. None of thisdisclosure suggests the use of the ascorbic acid and acetone as acarrier stream for the sample in a flow injection analysis method as inthe present invention, with the surprising advantages of lowertemperature and pressure for the step of hydrolysis conversion of thepolyphosphates to orthophosphate.

Hirai et al., J. Chromatogr., 206, 501-509 (1981), describe a flowinjection analysis method in which lower oxo acids of phosphorus such asphosphinate and phosphonate may be determined in addition toorthophosphate by oxidizing them in a solution of sodium hydrogensulfite and molybdenum(V)-molybdenum(VI).

Yoza et al., Anal. Chim. Acta, 121, 281-287 (1980), describe a flowinjection analysis method for the determination of polyphosphates [butonly pyrophosphate (P₂) and tripolyphosphate (P₃), whereas the method ofthe present invention can also determine hexametaphosphate (P₆)] whichcan be carried out at room temperature because it does not involvehydrolysis conversion of the polyphosphates to orthophosphate.Quantitative determination is made by measurement of the u.v.-absorptionof colored metal complexes of xylenol orange and methylthymol blue withthe polyphosphates.

Fogg et al., Analyst, 108, 1485-1489 (1983), describe the effect ofincreasing ethanol and acetone concentrations on the differential-pulsevoltammograms used in flow injection voltammetric determination of totalphosphate at a glassy carbon electrode. This method uses manualdigestion of polyphosphates, and further, would not be readily adaptableto process analysis.

Motomizu et al., Talanta, 30, 333-338 (1983), describe a flow injectionanalysis method for the determination of trace amounts of phosphate inriver water using a reaction with molybdate and Malachite Green inacidic medium to form a green species. This method measuresorthophosphate only at trace levels, and does not measurepolyphosphates.

Baba et al., J. Chromatogr., 295, 153-160 (1984), describe a paralleldetection flow injection system for the simultaneous determination ofphosphate and phosphonate. This method uses high pressure digestion anddual detection; whereas, the method of the present invention uses only asingle channel, and is therefore less expensive to operate.

Yoza et al., J. Chromatogr., 325, 385-393 (1985), describe a flowinjection analysis method for determination of inorganic polyphosphateswherein they are hydrolyzed by inorganic pyrophosphatase before reactionwith a molybdenum(VI) reagent for colorimetric determination. Thismethod is applicable only to P₃, P₂, and P₁ species; and enzymes areunstable and would not lend themselves to continuous on-line processanalysis.

Pauer, et al., Water SA, 14, 125-130 (1988), describe a flow injectionanalysis method for low concentrations of phosphate. The method uses tinchloride as a reducing agent and hydrazinium sulfate as a stablizer. Theeffects of injection volume, coil length and reagent concentration onoptimum sensitivity are evaluated.

Linares, et al., Anal. Chem., 58, 120-124 (1986) discloses analysis ofbinary and tenary mixtures of arsenite, arsenate and phosphate using aninjection valve; mixes molybdate and ascorbic acid prior to theirconfluence with the sample, which is said to yield higher peaks than twosequential confluence; and uses nitric acid instead of sulfuric acid.

Johnson and Petty, Anal. Chem., 54, 1185-1187 (1982) disclose a reverseflow injection analysis method in which a mixture of reagents (sulfuricacid, molybdate, ascorbic acid) are added to a sample stream; but onlyorthophosphate, apparently is analyzed.

SUMMARY OF THE INVENTION

In accordance with the present invention there is provided a flowinjection analysis method for determination by the molybdenum bluecomplex colorimetric reaction of total inorganic phosphate concentrationin an aqueous system containing dissolved inorganic polyphosphate aswell as orthophosphate, comprising the steps of (1) establishing afiltered sample stream from said aqueous system from which sample unitsmay be selected at designated intervals; (2) bringing together andadmixing on a continuous basis the following two reagent compositionstreams which then form the basic flow injection analysis stream: (a) acolor-forming reagent comprising an inorganic acid and molybdenum (V andVI), and (b) a reducing agent and preservative composition therefor; (3)interrupting the flow of reagent composition stream (b): a reducingagent and preservative composition therefor, and substituting thereforthe filtered sample stream of step (1) for sufficient time to select asample unit, which then becomes admixed with reagent composition stream(a): a color-forming reagent comprising an inorganic acid and molybdenum(V and VI); (4) restoring the flow of reagent composition stream (b);(5) heating the reaction mixture to 60°-95° C. for a sufficient time toeffect conversion of substantially all of the polyphosphate contained inthe sample unit to orthophosphate, said time also being sufficient toeffect the reaction of said orthophosphate with the molybdenum (V andVI) to form a color complex; and thereafter allowing said reducing agentto partially reduce the molybdenum (V and VI) so that it has an averageoxidation state between 5 and 6; (6) passing the reaction mixturecontaining the color complex through a colorimeter having a 600-850 nmfilter and reading the signal produced thereby; and (7) from the signalinformation and previously available standardization data, calculatingthe concentration of dissolved inorganic phosphates in the aqueousstream; wherein all of the above steps are carried out under a pressureof from 2-10 psi.

The present invention may also be set forth in the manner immediatelyfollowing, which describes in different terms the interaction of thesample unit and the reagent streams, which, while conceptually the sameas that described immediately above, may be viewed as different in termsof the different means for carrying out that interaction. A detaileddescription of those different means is provided further below.

In accordance with the present invention there is provided a flowinjection analysis method for determination by the molybdenum bluecomplex colorimetric reaction of total inorganic phosphate concentrationin an aqueous system containing dissolved inorganic polyphosphate aswell as orthophosphate, comprising the steps of (1) establishing afiltered sample stream from said aqueous system from which sample unitsmay be selected at designated intervals; (2) at one said designatedinterval, selecting a sample unit and injecting it as a discrete unitinto a continuously flowing reducing agent stream comprising a reducingagent and preservative composition therefor, so that the reducing agentstream is present in front of and behind said sample unit; (3) injectingthe sample unit and reducing agent stream into a color-forming reducingagent stream comprising an inorganic acid and molybdenum (V and VI) insuch manner that the sample unit and color-forming reagent arethoroughly admixed while bounded in front and behind by said reducingagent stream; (4) heating the reaction mixture to 60°-95° C. for asufficient time to effect conversion of substantially all of thepolyphosphate contained in the sample unit to orthophosphate, said timealso being sufficient to effect the reaction of said orthophosphate withthe molybdenum (V and VI) to form a color complex; and thereafterallowing said reducing agent to partially reduce the molybdenum (V andVI) so that it has an average oxidation state between 5 and 6; (5)passing the reaction mixture containing the color complex through acolorimeter having a 600-850 nm filter and reading the signal producedthereby; and (6) from the signal information and previously availablestandardization data, calculating the concentration of dissolvedinorganic phosphates in the aqueous stream; wherein all of the abovesteps are carried out under a pressure of from 2-10 psi.

The novel interaction of the sample unit and reagent streams in themethod of the present invention creates a facile process which permitsconversion of the various polyphosphates to orthophosphate anddevelopment of the molybdate (V) color reaction while being carried outat 60°-95° C. and under 2-10 psi. Thus, the method of the presentinvention utilizes temperatures below the boiling point of water, i.e.,<100° C. and significantly lower pressures than has been the caseheretofore, with the attendant advantages described further below.Accordingly, it is now possible, using the method of the presentinvention, to develop inexpensive on-line process analyzers which permitregular and reliable determination of inorganic phosphateconcentrations.

Thus, the present invention further relates to an apparatus for flowinjection analysis (FIA) determination by the molybdenum blue complexcolorimetric reaction of total inorganic phosphate concentration in anaqueous system containing dissolved inorganic polyphosphate as well asorthophosphate, comprising (1) filter means and three-way valve meansfor establishing a filtered, continuously flowing sample stream fromsaid aqueous system to waste, from which sample units may be selected atdesignated intervals; (2) mixing valve means having two switchable modesof operation: (a) when a sample unit is not to be analyzed, two reagentcomposition streams comprising a color-forming reagent and a reducingagent, are brought together and admixed on a continuous basis; and (b)when a sample unit is to be analyzed, the stream of reducing agent isinterrupted and the filtered sample stream is substituted therefor forsufficient time to select a sample unit, which then becomes admixed withthe color-forming reagent stream, after which the flow of the reducingagent stream is restored; (3) a first conduit means for separatelyconnecting and carrying the sample stream and the two reagentcomposition streams to said mixing valve means; (4) container means forthe two reagent compositions, connected to said mixing valve means bysaid first conduit means; (5) a second means from said mixing valvemeans, and eventually to waste, for carrying the reaction mixture streamformed by mixing of the sample stream and the two reagent compositionstreams during and subsequent to passage through said mixing valvemeans, said second conduit means being of sufficient length to permitcompletion of the colorimetric reaction in the reaction mixture stream;(6) heating means through which the second conduit means passes forheating of the reaction mixture stream; (7) colorimetric means throughwhich the second conduit means passes, having a 600-850 nm filter forreading the signal produced by the reaction mixture stream; and (8)means for maintaining a pressure of from 2-10 psi throughout the meanscomprising the FIA apparatus, whereby the sample, reagent composition,and reagent mixture streams are individually and collectively impelledthrough said means, eventually to waste.

In particular, the present invention relates to the FIA apparatusdescribed above wherein the filter means is a tangential flow bypassmembrane filter system; the heating means is an immersion heater; thefirst and second conduit means are made of polyetheretherketone tubing;and the FIA apparatus additionally includes computer means which processthe data from the colorimeter means together with other data whichresults in calculation of the concentration of total inorganic phosphatecontained in the aqueous system from which the sample for testing wasobtained.

The present invention also further relates to an apparatus for flowinjection analysis (FIA) determination by the molybdenum blue complexcolorimetric reaction of total inorganic phosphate concentration in anaqueous system containing dissolved inorganic polyphosphates as well asorthophosphate, comprising (1) filter means, selector valve means, andinjection valve means for establishing a filtered, continuously flowingsample stream from said aqueous system to waste, from which sample unitsmay be selected at designated intervals for passage through the FIAapparatus, by switching of the injection valve means; (2) injectionvalve means and separate mixing connector means which are connected andoperate together so as to have two switchable modes of operation: (a)when a sample unit is not to be analyzed, two reagent compositionstreams comprising a color-forming reagent and a reducing agent, arebrought together and admixed on a continuous basis at and by the mixingconnector means, the color-forming reagent flowing directly into saidmixing connector means, and the reducing agent flowing into said mixingconnector means after first passing through said injection valve means;and (b) when a sample unit is to be analyzed, the stream of reducingagent is interrupted by switching of said injection valve means and thefiltered sample stream is substituted therefor for sufficient time toselecta sample unit, which then becomes admixed, at said mixingconnector means, with the color-forming reagent stream, after which theflow of the reducing agent stream is restored by switching of saidinjection valve means; (3) a first conduit means for separatelyconnecting and carrying the sample stream and the reducing agent streamto said injection valve means and from there to said mixing connectormeans; and a second conduit means for connecting and carrying thecolor-forming reagent stream to said mixing connector means; (4)container means for the two reagent compositions, connected to theinjection valve means and the mixing connector means by said first andsecond conduit means as set out above; (5) a third conduit means fromthe mixing connector means and eventually to waste, for carrying thereaction mixture stream formed by mixing of the sample stream and thetwo reagent composition streams during and subsequent to passage throughsaid mixing connector means, said third conduit means being ofsufficient length to permit completion of the colorimetric reaction inthe reaction mixture stream; (6) heating means through which the thirdconduit means passes for heating of the reaction mixture stream; (7)colorimetric means through which the third conduit means passes, havinga 600-850 nm filter for reading the signal produced by the reactionmixture stream; and (8) means for maintaining a pressure of from 2-10psi throughout the means comprising the FIA apparatus, whereby thesample, reagent composition, and reaction mixture streams areindividually and collectively impelled through said means, eventually towaste.

In particular, the present invention relates to the FIA apparatusdescribed above wherein the filter means is a targeted flow bypassmembrane filter system; the heating means is an immersionheater; thefirst, second and third conduit means are made of polyetheretherketone(PEEK) tubing; the mixing connector means is a T-connector; and the FIAapparatus additionally includes computer means which process the datafrom the colorimeter means together with other known data which resultsin calculation of the concentration of the total inorganic phosphatecontained in the aqueous system from which to sample for testing wasobtained.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram of the apparatus with the preferred embodiment ofthe selector valve and injection valve.

FIG. 2 illustrates the 3-way valve and mixing valve, alternatives to theselector and injection valves of FIG. 1.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a method and apparatus for flowinjection analysis, a technique well known in the art. Such a method andapparatus requires a continuous flow of a sample/reagent stream in whicha color reaction product is formed and read on a colorimeter. Such amethod is typically carried out in an apparatus comprising a closedsystem in which the sample/reagent stream is carried in conduit meansconsisting of tubing of suitable dimensions and materials. Thecontinuous movement of the sample/reagent stream is produced by apositive pressure accomplished by any suitable means, for examplepumping means, such as a peristaltic pump, or a pressurized system inwhich compressed air or an inert gas such as nitrogen is used to propelthe sample/reagent stream through the tubing and other apparatus meansused to carry out the method. A pressurized system using compressed airis preferred. The pressure is maintained not only by the pressure of thegas source imposed on the entire system, but also by the use incombination therewith of pressure regulators, restrictor coils withreduced internal diameters, backpressure loops functioning in the sameway, and the use of a semipermeable membrane through which thesample/reaction stream passes in order to remove entrained air. The useof any one or more of these devices in combination readily maintains thedesired pressure throughout the flow injection analysis system.

The tubing which is used to carry the sample stream, as well as thereagent composition streams and reaction mixture invention, must becomposed of a material which is able to withstand the rather harshconditions to which it is continually subjected during the method of thepresent invention, including low pH, elevated temperatures and strongreagents, while maintaining dimensional uniformity within very stricttolerances, which is essential for assuring consistency andreproducibility of the analytical results over a long period of time.Materials which are subject to swelling, distention, elongation or otherchanges in dimensional uniformity may not be suitable for the tubingused in the apparatus of the present invention. For example, whilepolytetrafluoroethylene (PTFE) has many desirable features, it lacks thehigh degree of dimensional uniformity after extended use required forthe method of the present invention. Polyethylene does not possesssufficient resistance to the low pH and reagents present in the presentmethod. A material which has been found suitable, on the other hand, ispolyetheretherketone (PEEK), and it is preferred for use with theapparatus of the present invention.

The size of the tubing is selected so as to accomplish a desired flowrate with respect to a sample size within a desired range, which makeseconomic use of the required reagents and affords an adequate reactiontime. In the method and apparatus of the present invention, it has beenfound useful to employ tubing having an internal diameter (ID) of from0.0125 to 0.1000 cm, with an internal diameter of 0.0500 cm (=0.02 in)being preferred.

Using tubing having the preferred 0.0500 cm internal diameter, a flowrate throughout the flow injection system of between 0.13 and 0.18mL/min is maintained, preferably 0.15 mL/min. With such a flow rate, thesample unit size may vary between 10 and 150 μL, preferably between 50and 125 μL, and most preferably 100 μL. With increasing sample unitsize, it has been found that there is increasing difficulty inmaintaining adequate acidity to prevent silica (SiO₂) interference.Silica undergoes the same color-forming reaction with the molybdatereagent employed in the method of the present invention as doesorthophosphate, and thus creates the possibility of interference withthe total inorganic phosphate determination. Because the color-formingreaction with silica is pH dependent, it is possible to virtuallyeliminate the silica interference by maintaining a sufficiently low pH.This is done most conveniently by utilizing an adequate amount of theinorganic acid, e.g., concentrated sulfuric acid, which is part of thecolor-forming reagent composition used in the method of the presentinvention.

The pressure in the system, which is preferably achieved by use ofcompressed air to create a pressurized system, and by means of which theflow rate described above is maintained, should be between 2 and 10 psi,preferably between 4 and 6 psi. This is a significant reduction in theamount of pressure required in many flow injection analysis methods anddevices employed in the prior art, which have often used pressures ashigh as 70 psi. The purpose of such high pressures was to suppress thebubbling caused by the release of dissolved air in the sample/reactionmixture during travel through the colorimeter, which interfered with thereadings obtained from that instrument. Such high pressures were aconcomitant, however, of the use of high temperatures, i.e., >100° C.,in the prior art methods to carry out the hydrolysis reaction whichconverted the polyphosphates to orthophosphates. It is possible, usingthe present invention, to avoid the high pressures of the prior artmethods and devices because the corresponding high temperatures of thosemethods and devices have also been eliminated.

Returning to the starting point of the flow injection analysis method ofthe present invention, it is one for the determination of theconcentration of total dissolved inorganic phosphate in an aqueoussystem. It has already been noted further above that the inorganicphosphate content is primarily polyphosphate. It has also been notedthat the method of the present invention may be used to determine theconcentration of orthophosphate only, if that is desired.

The aqueous system in its broadest context is any water solutioncontaining dissolved inorganic phosphate which is used as a sample foranalysis in the flow injection method of the present invention. Mosttypically, this aqueous system is water from a cooling tower or aboiler. However, the method of the present invention obviously has widerapplicability, and it is intended that it include analyses where theaqueous system is, e.g., a clinical specimen, or where a sample offertilizer has been dissolved in water for analysis using the method ofthe present invention.

Where the aqueous system sample is from cooling tower water or boilerwater, it is usually found to contain suspended fine solids which willclog the tubing and otherwise interfere with the various pieces ofapparatus used to carry out the method of the present invention. Thus,sample filtration is necessary to separate corrosion inhibitingphosphate from phosphate tied to suspended material and to preventplugging of the instrument. Scale and corrosion inhibiting phosphate isconsidered to be dissolved phosphate or phosphate attached to <0.45μsized particles. Bypass membrane filtration is preferred, withtangential entry of bypass being desirable for on-line samplefiltration, because membrane fouling is slowed by the cleaning action ofthe sample stream. Commercial filtering systems which are suitableinclude the from Millipore Corp., Bedford, Mass. 01730-9903; Minitan-Sfilter assembly, Collins Products Company, Livingston, Tex. 77351 andthe Collins Swirlclean bypass filter. Consequently, it is provided thatthe sample stream be filtered. Any filter material or device which willremove the suspended fine solids from the sample stream is suitable; andit has been found that good results are achieved with the method andapparatus of the present invention when particles of 0.45μ and largerare removed.

It is necessary to establish the filtered sample stream in such a waythat sample units may be selected therefrom at designated intervals.This is suitably carried out using a selector valve together with aninjection valve, both of which are of known design and allow the samplestream, which is being filtered, to flow in a continuous manner throughthe selector and injection valves to waste, but not through any otherpart of the flow injection analysis system. In addition to assuring thata fresh sample unit is provided whenever a sample is to be analyzed, theselector valve also functions to permit the introduction of standardsand distilled water into the basic flow injection analysis stream. Itwill be appreciated that other devices may be substituted for theselector valve, i.e., devices of known design and function which arecapable of carrying out the method of the present invention,particularly that part of the method accomplished by the selector valve.One such other device is described further below.

Sample units for evaluation in the flow injection system are selected atdesignated intervals. These designated intervals are predetermined basedon the number of samples that it is desired to test within a givenperiod of time, and are usually preprogrammed into a computer or similardevice which controls the operation of the entire flow injectionanalysis system. During conventional operation, the selector valve willbe set so that the sample stream enters the selector valve and then goeson to the injection valve, and from there on to waste. On command fromthe computer or other control device, or even manually, the injectionvalve then directs the sample stream through a sample loop of tubingwhich is of the appropriate dimensions to give the desired sample size,most preferably 100 μL.

The sample loop is preferably in the separate device termed theinjection valve, which has as its function the injecting of the sampleunit into the continuously flowing reagent stream. The device functionsin such a way that the sample unit is injected into a reagent stream.The injection of the sample unit into a reagent stream may take place intwo different ways which, while accomplished by different means, areconceptually the same and thus represent different embodiments of thepresent invention. One such means is a mixing valve, which has two ormore inlet ports and a single outlet port. Within the valve assembly,means controlled by the operation of a solenoid allow measuredquantities of the contents of a tube leading to one of the inlet portsto pass through the valve assembly and out the outlet port. The solenoidthen closes that inlet port and opens a second inlet port, where again ameasured quantity of the contents of a tube leading to the second inletport are allowed to pass through the valve assembly and out the outletport. By alternating the opening and closing of these inlet ports, e.g.,once a second, a thorough mixing of the contents of the two tubesentering the inlet ports is achieved.

When a mixing valve is used to carry out the method of the presentinvention, it functions in the following way. During the stage of theprocess when the basic flow injection analysis stream is moving throughthe system in a state of readiness to receive a sample unit to beanalyzed, the two reagent composition streams which form the basic flowinjection analysis stream are brought together and admixed at a mixingvalve. These two reagent composition streams are (a) the color-formingreagent compromising an inorganic acid and molybdenum (V and VI), and(b) the reducing agent and preservative composition therefor. Either thetiming of the solenoid which controls the amount of each reagent streamleaving the outlet port, or the concentrations of the reagentcompositions themselves, may be adjusted so as to predetermine the ratioof the reagent concentrations in the basic flow injection analysisstream. These can be set as desired, depending on the makeup andstoichiometry of the reagent composition streams. For example, whereconcentrated sulfuric acid and ascorbic acid are used, the timing and/orconcentrations are adjusted to provide a 1:1 molar ratio of thereagents.

When a sample unit is to be analyzed, the selector and injection valvesare set and activated so that a sample unit travels through a tube to athird inlet port of the mixing valve described above, where it entersthe mixing valve. At the same time, however, the inlet port for thereducing agent and preservative composition is closed, so that thesample unit is, in effect, substituted therefor, and as a consequence,the sample unit becomes admixed with the color-forming reagent which isstill entering the mixing valve. After the sample unit has completelypassed through the mixing valve, its inlet port is closed and that forthe reducing agent and preservative is reopened. As a consequence of theabove actions, it will also be seen that the reducing agent andpreservative reagent composition is present in front of and behind thesample unit in the basic flow injection analysis stream.

Another embodiment of the present invention replaces the selector andinjector valves described above with the simple expedient of a three-wayvalve connected by tubing directly to the mixing valve, through whichsample continuously flows to waste through one of the ports of thethree-way valve. By means of such a valve, it is possible to have acontinuous flow of fresh sample, and then by switching the three-wayvalve, provide for direct flow of a sample unit to the mixing valve, theunit size being determined by the length of time that the three-wayvalve remains open for passage of sample.

Another means for accomplishing the injection of the sample unit into areagent stream, involves the use of an injection valve as describedabove together with a T-connector. As with the mixing valve embodiment,during the stage of readiness for receiving a sample unit, the tworeagent streams are mixed together on a continuous basis, but by meansof being brought together at the T-connector rather than through amixing valve. When a sample unit is to be analyzed, the injection valveis activated and the sample unit is injected into the reducing agent andpreservative composition reagent stream, which also passes through theinjection valve on a continuous basis. As a consequence, the reducingagent stream is present in front of and behind said sample unit, viewedas a continuously flowing system, just as with the mixing valveembodiment described further above. The reducing agent stream pushes thesample unit on ahead of it so that when the sample unit reaches theT-Connector, only sample and color-forming reagent are admixed at theT-connector, just as with the mixing valve embodiment described furtherabove.

In both embodiments described above, as the sample/color-forming reagentmixture passes through the remainder of the flow injection analysissystem, acid hydrolysis of inorganic phosphate to orthophosphate takesplace and the molybdate heteropoly yellow complex is formed. During thecourse of this passage, the reducing agent will also completelyinfiltrate the mixture, forming the molybdate heteropoly blue complex.It is believed that by means of this novel series of steps, the methodof the present invention is able to utilize low pressures andtemperatures to accomplish the hydrolysis of dissolved polyphosphatesand the color-forming reaction, which has required high temperatures andpressures in the methods of the prior art.

In both of the two embodiments for carrying out the method of thepresent invention, the reducing agent stream comprises a reducing agentand a preservative composition therefor. The reducing agent acts toreduce the phosphomolybdate complex to the heteropolymolybdate blueform. A commonly employed reducing agent recognized for this purpose isascorbic acid, and this is the preferred reducing agent for use in themethod of the present invention. However, other reducing agents areknown in the art, and any of these, or any combination of these, may beemployed. See, e.g., Frenzel, Fresenius' Z. Anal. Chem., 329, 668(1988); Standard Methods for the Examination of Water and Wastewater,Clesceri et al., eds. 17 Edition, p. 4-175 to 4-176 (1989): and Pedersonet al., Analytical Chemica Acta, 238, 191 (1990). Suitable reducingagents include stannous chloride.4-amino-3-hydroxy-1-naphthalenesulfonic acid, sodium sulfite, sodiumbisulfite, and sodium metabisulfite. The amount of ascorbic acidemployed will be between 10 and 30 g/L, preferably between 15 and 20g/L.

It is possible to use a catalyst such as antimony (III) to acceleratethe activity of the reducing agent, and thus the rate of reduction.

Decomposition of the reducing agent such as ascorbic acid will occurwithout the use of one or more preservatives. Such decomposition can becaused by dissolved oxygen in the aqueous system, or by the presence ofoxygen radicals. The presence of heavy metals may also catalyze suchdecomposition. Preservative agents for use with the reducing agents ofthe present invention, and which act as oxygen scavengers, include thoserecognized in the art as suitable for that purpose, e.g., acetone, whichis preferred, other ketones such as methylethyl ketone, glycerol (Kondoet al., Corr. Eng., 36, 235, 1987), and glycol. They may be used aloneor together in combination.

Chelating agents which bind to heavy metals capable of catalyzing thedecomposition of the reducing agents may also be used in thepreservative composition. Any chelating agent which will chelate metalswhich cause instability of the ascorbic acid, and which is otherwisecompatible with the other elements present in the method of the presentinvention, may be used. A preferred chelating agent isethylenediaminetetraacetic acid (EDTA) in any of its various salt forms,e.g., tetrasodium EDTA, edetate sodium, edetate disodium, edetatetrisodium, and edetate calcium disodium. Disodium EDTA is preferred.Nitrilotriacetic acid may also be used, for example.

A preferred reducing agent and preservative composition for use in themethod of the present invention has the following composition:

    ______________________________________                                        17.6    g        ascorbic acid   In 1 L of                                    50      mL       acetone         deionized                                    7.6     mg       disodium EDTA   water                                        ______________________________________                                    

The disodium EDTA is conveniently added as 2 mL of Calgon ReagentR-5010, which is 0.001M EDTA and contains sufficient NaOH to solubilizethe EDTA, as well as a very small quantity of a preservative.

The amount of reducing agent such as ascorbic acid employed will bebetween 10 and 30 g/L, preferably between 15 and 20 g/L. The amount ofpreservative such as acetone employed will be between 45 and 55 mL/L,preferably 50 mL/L.

In both embodiments of the method of the present invention describedabove, the color-forming reagent stream comprises an inorganic acid andmolybdenum (V and VI). Hydrolysis of the polyphosphate to orthophosphatetakes place in an acidic medium, and for this purpose there may beemployed, e.g., concentrated sulfuric acid (H₂ SO₄), which is preferred.Other suitable inorganic acids, such as hydrochloric acid (HCl) andperchloric acid (HClO₄) may be used, but these tend to be more volatileand fuming and/or oxidizing, as in the case of HClO₄, which tends tointroduce some element of hazard into the flow injection analysismethod. Nitric acid (HNO₃) may also be employed, either alone or incombination with H₂ SO₄. However, since HNO₃ acts as an oxidizing agent,it can introduce complications into the overall chemistry of the flowinjection analysis method.

The inorganic acid reagent, while its purpose is hydrolysis of thepolyphosphate to orthophosphate, is referred to herein along with themolybdenum (V and VI) as the color-forming reagent, since these reagentsare most advantageously and typically employed together.

The molybdenum blue complex reagent composition may be prepared inaccordance with procedures known in the art. However, the method of thepresent invention does permit use of a simple molybdate reagent which isa distinct improvement over the complex molybdate reagent used by Hiraiet al., and prepared as described in Anal. Chim. Acta, 115, 269-277.That procedure involves several steps and use of concentratedhydrochloric acid in addition to concentrated sulfuric acid, as well asuse of a zinc reducing agent. By contrast, the molybdate reagent for usein the method of the present invention may be prepared simply bydissolving from 5 to 15 g, preferably 10 g of ammonium molybdatetetrahydrate [(NH₄)₆ Mo₇ O₂₄ •4H₂ O] in from 60 to 120 mL, preferably102 mL of concentrated (95%) sulfuric acid (H₂ SO₄). The solution maythen be diluted to 1 L with deionized water to give the molybdenum (Vand VI) reagent solution. When this reagent mixes with the reducingagent stream containing, e.g., ascorbic acid, the ascorbic acidpartially reduces the molybdenum so that it has an average oxidationstate between 5 and 6. The molybdenum blue color complex results.

The manner in which the color-forming reagent solution is brought intocontact with the sample unit and reducing agent stream has already beendescribed. All of these components must be thoroughly admixed to formthe resultant reaction mixture in the course of their passage throughthe tubing of the flow injection analysis system. This can beaccomplished by having the tubing carrying the sample unit and carrierstream mixture meet tubing carrying the reagent solution at a 90° angleT-connector. Other devices which accomplish the same objective ofthorough admixture may be used. One such device, which retains theadvantages of efficiency, reliability, and economy that characterize theT-connector, is a solenoid operated mixing valve of the type sold byBio-Chem Valve Corp., East Hanover, N.J. Such mixing valves feature lowpower consumption, isolated solenoid, high cycle life, low internalvolume, fast response time, Teflon wetted parts, and valve seat travelsadjusted for accurate fluid sampling. The mixing valve can mix togetherthe proper ratio of reagents and samples by switching from one stream toanother in rapid succession, resulting in a well mixed solution. Thevery rapid mixing of samples and reagents which can be achieved withsuch a mixing valve results in faster reaction times and sharper peakshape from the colorimeter.

The next step involves heating of the reaction mixture so that thehydrolysis of the inorganic polyphosphates to orthophosphates may becompleted. This hydrolysis or digestion step is carried out at atemperature of from 60°-95° C., and preferably from 75°-93° C., but mostpreferably at 90° C. Where it is desired to analyze only the content oforthophosphate in the aqueous system, then the temperature will bebetween 25° and 35° C., preferably 30° C. The time for this step to becompleted, whether it is for total inorganic polyphosphate, ororthophosphate only, will be from 10 to 25 min, usually from 15 to 20min. A typical residence time for completion of this step is 16 min. Thedevice most convenient for carrying out this step is a simple reactioncoil, e.g., one coil of tubing 1000 cm in length and 0.0500 cm (=0.02in) internal diameter encased in an aluminum heater block.

Using flow rates within the range of those described above, the desiredoverall reaction time is achieved with such a device. Other means may besubstituted for the reaction coil. It may be more economical, e.g., tochange from a spool of tubing encased in an aluminum heater block to animmersion heater with a thermocouple attached to the surface of theheater and held in place by tightly rapped tubing and insulated withsilicon tape. In such a device, the surface of the heater is hotter thanthe opposite side of the tubing by about 5° C. (heater surfacetemperature of about 90° C. and room temperature operation), making thesample temperature somewhere between those two values. Using moreinsulation reduces the temperature differential, but slows coolingrates. Using this design, heater temperatures up to about 95° C. willnot boil the flow injection analysis reaction mixture.

As has already been described, the reaction which takes place in thisstep achieves two results: (1) the inorganic polyphosphates areconverted by acid hydrolysis to orthophosphate, and (2) theorthophosphate reacts with the molybdenum (V and VI) reagent to form theheteropoly blue complex. This latter reaction is the color-forming stepin which the color complex is formed. A third and ancillary reaction mayalso be taking place during this step; and that is completion of thepartial reduction of the molybdenum (V and VI) by the reducing agent,e.g., ascorbic acid so that an average oxidation state between 5 and 6is achieved.

Even though the reaction temperatures for the step described above arebelow the 100° C. boiling point of water, and it is therefore unlikelythat significant amounts of dissolved air gases (oxygen and nitrogen)will come out of solution, it is preferred to employ an air filter whichwill remove any such bubbles of gas which may unexpectedly appear. Theevolution of gas bubbles can cause unacceptable detector "noise" whenthe reaction mixture containing the color complex is passed through thecolorimeter for reading. As already explained above, the air filter isconveniently a semipermeable membrane through which the reaction mixtureis passed to remove any extraneous gases which have formed. Such airfilters are well known in the art. Furthermore, because of theimprovement obtained with the method of the present invention wherebylower temperatures and pressures are required than with the methodsemployed heretofore in the prior art, it is not necessary to employ atthis stage of the method a cooling coil to reduce the temperature of thereaction mixture prior to passing it through a colorimeter.

The next step in the flow injection analysis method of the presentinvention involves passing of the reaction mixture containing the colorcomplex through a colorimeter. This is typically a flow-through cellspectrophotometer equipped with a filter which permits monitoring of theheteropoly blue complex within a wavelength range of from 600 to 850 nm.A 650 nm filter is usually employed. The path length for theflow-through colorimeter cell is from 0.5 to 2 cm, but is preferably 1cm in length.

The last step of the flow injection analysis method of the presentinvention is the one which utilizes the information obtained from thecolorimeter reading in the preceding step and together with informationalready available, calculates the concentration of total inorganicphosphate contained in the aqueous system from which the sample fortesting was obtained. It is desirable to employ standards and routinelytest these so as to obtain and have readily available 2-pointstandardization data. It is most convenient to employ a computer toprocess all of this data and calculate the desired end result. Thus, thesignal from the colorimeter may be sent directly to such a computer; andthe information derived from the colorimeter reading together with theother data necessary to calculate the end result which is already storedin the computer memory, permits a very rapid and automatic readout ofthe concentration of total inorganic phosphates in the aqueous system onan ongoing and regular basis.

DESCRIPTION OF THE DRAWINGS

FIG. 1 of the drawings depicts a typical analyzer apparatus for carryingout the method of the present invention. The solid lines depict conduitmeans, i.e., tubing which carries the sample/reaction streams throughthe various steps of the method. The depiction is not drawn to scale,and the length of tubing may be varied unless a preferred length isotherwise specified.

The dashed lines enclose specific means in the apparatus which arereplaced with other means to form the embodiment shown in FIG. 2. Asample stream 1 from an aqueous system (not shown) enters through afilter means 3 which removes suspended solids which might otherwise clogthe tubing of the system.

The sample stream continuously flows through the selector valve 5, towhich standard solutions 7 and 9 are also connected by tubing 15 and 17,respectively. These standard solutions operate as substitutes for thesample stream and are sent through the flow injection system on aregular basis in order to provide a set of 3-point standardization datafor making the end result calculations.

Movement of the standard solutions as well as the sample stream isaccomplished by use of a pressurized system, using a source ofcompressed air 11 under pressure regulated by regulator 13.

When a sample is analyzed, the selector valve 5 will be directing thesample stream through a sample loop 23 in injection valve 21 throughtubing 55 to waste, thus assuming a continuous supply of fresh sample.At designated intervals, the injection valve 21 switches the samplein-line so that the reducing agent reagent 25 arriving through tubing 27and previously contained in loop 23 of injection valve 21, pushes thesample unit ahead through tubing 29. Before the sample is injected,reducing agent reagent 25 flows through loop 23 and tubing 29 on acontinuous basis, where it becomes admixed at T-connector 35 withcolor-forming reagent 31.

The pressurized containers for the standard solutions 7 and 9, as wellas the reagents 25 and 31, are assisted in their function by checkvalves, in-line filters, and restrictor coils, but these are standardfeatures and are not identified by numbers in the drawing.

While the sample unit is traversing tubing 29, it is bounded in frontand behind by reducing agent reagent 25. This sample unit enters theT-connector 35, into which also enters tubing 33 carrying thecolor-forming reagent 31. Because of the "T" configuration of thejunction, there results a thorough admixture of the sample unit andcolor-forming reagent. When the reducing agent infiltrates thisadmixture, the overall reaction mixture comprising the basic flowinjection analysis stream is formed.

The reaction mixture is carried through tubing 37 to a heating device 39which maintains a temperature between 60° and 95° C., and which containsa coil of tubing 41 of sufficient length to allow the required residencetime of about 16 min for the reaction mixture.

The heteropoly blue complex has now been formed in the reaction mixture,and this is carried through tubing 43 and an air filter 45 to remove anyair bubbles which have unexpectedly evolved during the reaction heating.Instead of an air filter 45, there may be employed at this point abackpressure loop 46.

The color complex together with the reaction mixture is now carriedthrough tubing 47 to the colorimeter 49 containing a flow-through cellwith a 650 nm filter (not shown), where the sample is read. The readingof the colorimeter 49 may be visually inspected, or may form a signalsent to a computer (not shown) which uses that and other data tocalculate the concentration of inorganic polyphosphate in the sample.

A restrictor coil 51 assists in maintaining the pressure (@ 5 psi) inthe system, and after passing through this coil, the reaction mixturewith color complex which has now been read in the colorimeter 49, passesto waste through tubing 53.

FIG. 2 of the drawings depicts another embodiment of the apparatus ofthe present invention in which a three-way valve and mixing valve meanshave been substituted for the selector valve and injection valve meansdepicted in FIG. 1 of the drawings. The area of substitution is shown inFIG. 1 by means of the dashed lines. While the different means of FIG. 2operate in a different way from the means of FIG. 1, conceptually thesame functional results are obtained, i.e., the same method steps areachieved.

The filtered sample stream 1 enters a three-way valve means 60 and flowsthrough conduit means, i.e., tubing 62 to waste on a continuous basis soas to provide fresh sample. When a sample is to be analyzed, thethree-way valve 60 is switched so that a sample unit now flows throughtubing 64 and pressure regulator 66 to the mixing valve means 68. Thesize of the sample unit is determined by the length of time that thethree-way valve 60 remains switched, which is readily controlled in apredetermined manner.

The sample unit in tubing 64 enters mixing valve 68 through inlet port70 and then exits the mixing valve through outlet port 72. The amount ofsample which enters and leaves the mixing valve is determined by theopening and closing of the inlet port 70, the operation of which, inturn, is controlled by solenoid 74. Once the sample leaves the mixingvalve 68, it continues on through tubing 37 to the heater 39 and otherportions of the flow injection analysis system depicted in FIG. 1 of thedrawings.

During the stage of the process when the basic flow injection analysisstream is moving through the system in a state of readiness to receive asample unit to be analyzed, the two reagent composition streams whichform the basic flow injection analysis stream are brought together andadmixed by the mixing valve 68. The reducing agent and preservativecomposition reagent 25 moves through tubing 27 (as in FIG. 1) to inletport 76 controlled by solenoid 78. The color-forming reagent 31 movesthrough tubing 33 (as in FIG. 1) to inlet port 80 controlled by solenoid82. Thorough admixing of the two reagents is accomplished by the mixingvalve 68 through rapid successive opening and closing of the inlet ports76 and 80, controlled by solenoids 78 and 82, respectively. Thethoroughly admixed reagents then exit the mixing valve through outletport 72 and continue on through the remainder of the flow injectionanalysis system by way of tubing 37.

When the sample unit enters the mixing valve 68 through its inlet port70, inlet port 76 for reducing agent 25 is automatically closed bysolenoid 78 in accordance with a preset control program (not shown). Asa result, the sample unit now becomes admixed with the color-formingreagent 31 by operation of the mixing valve 68 as described above. Assoon as the sample unit has passed through the mixing valve, its inletport 70 is closed again and inlet port 76 for reducing agent 25 isautomatically reopened by the same preset control program. As a result,the reducing agent 25 will be found in front of and behind the mixtureof sample unit and color-forming reagent, and these all together formthe basic flow injection analysis stream which proceeds on throughtubing 37 to the remaining steps and means of the flow injectionanalysis system depicted in FIG. 1.

Mixing valve 68 depicted in FIG. 2 has a total of six inlet ports, thefunction of only three of which has been described above. Use of theadditional inlet ports can provide a facile substitute for the selectorvalve and injection valve depicted in FIG. 1 with respect to the use ofstandards and dilution with distilled water as well. When it isnecessary to analyze the standards 7 and 9, they may be brought tomixing valve 68 through tubing 15 and 17, respectively (as in FIG. 1),and enter through inlet ports 84 and 86 controlled by solenoids 88 and90, respectively. Their admixture with the reagents 25 and 31 takesplace in the same manner as described above for the sample unit, all ofwhich is controlled by the preset control program. Use of the remaininginlet port 92 controlled by solenoid 94 for introduction of distilledwater through tubing 98 which passes through pressure regulator 100,affords a ready means of direct dilution of any of the samples,standards or reagents which enter the mixing valve 68, as describedabove.

The remainder of the flow injection analysis system and its function areas described further above for FIG. 1.

DESCRIPTION OF PREFERRED EMBODIMENTS

The following example provides a demonstration of a preferred embodimentfor carrying out the method of the present invention, but is notintended to be in any way a limitation of that method.

A filtered cooling water stream runs to a selector valve. At designatedintervals the selector valve directs the sample stream through a 10 μLsample loop in an injection valve. The injection valve switches thesample in-line so that the ascorbic acid reagent (carrier) pushes thesample ahead. The sample mixes with acid molybdate at a 90° angleT-connector. From there it enters a 1000 cm 0.02 in id heating coil at60°-80° C. For determination of orthophosphate only, the heating coilwas at 30° C. It takes 16 min for the sample to traverse the coil. Itthen passes through an air filter which removes extraneous air bubbles.Next the sample flows through a colorimeter with 1 cm path length and650 nm filter. The signal is sent to a computer which calculates thedata from a 2-point standardization which is repeated periodically byinjecting orthophosphate standards.

The following table of values shows results obtained using the abovemethod for cooling water, except that the sample stream was sampledindividually through a sampling device rather than an incoming stream toa selector valve.

                  TABLE                                                           ______________________________________                                        Sample   mg/L    mg/L      Sample                                                                              mg/L  mg/L                                   No.      Total   Ortho     No.   Total Ortho                                  ______________________________________                                        3127     <2      <2        3265  3.8   2.6                                    3266     2.7     <2        3288  <2    <2                                     3289     5.5     4.3       3425  2.4   <2                                     3275     8.2     4.0       3276  20.7  12.2                                   3491     <2      <2        3653  4.3   3.6                                    3767     16.4    4.2       3768  17.4  5.5                                    3692     44.4    27        3892  8.2   4.7                                    3771     16.6    2.4       3279  28.9  13.3                                   ______________________________________                                    

What is claimed is:
 1. An apparatus for flow injection analysis (FIA)determination by the molybdenum blue complex colorimetric reaction oftotal inorganic phosphate concentration in an aqueous system containingdissolved inorganic polyphosphate as well as orthophosphate, comprising(1) filter means and three-way valve means for establishing a filtered,continuously flowing sample stream from said aqueous system to waste,from which sample units may be selected at designated intervals; (2)mixing valve means having two switchable modes of operation: (a) when asample unit is not to be analyzed, two reagent composition streamscomprising a color-forming reagent and a reducing agent, are broughttogether and admixed on a continuous basis; and (b) when a sample unitis to be analyzed, the stream of reducing agent is interrupted and thefiltered sample stream is substituted therefor for sufficient time toselect a sample unit, which then becomes admixed with the color-formingreagent stream, while bounded in front and behind by said reducing agentstream when the flow of the reducing agent stream is restored, therebyforming a reaction mixture of the sample unit, color-forming reagent andreducing agent; (3) a first conduit means for separately connecting andcarrying the sample stream and the two reagent composition streams tosaid mixing valve means; (4) container means for the two reagentcompositions, connected to said mixing valve means by said first conduitmeans; (5) a second conduit means from said mixing valve means, andeventually to waste, for carrying the reaction mixture stream formed bymixing of the sample stream and the two reagent composition streamsduring and subsequent to passage through said mixing valve means, saidsecond conduit means being of sufficient length to permit completion ofthe colorimetric reaction in the reaction mixture stream; (6) heatingmeans through which the second conduit means passes for heating of thereaction mixture stream; (7) colorimetric means through which the secondconduit means passes, having a 600-850 nm filter for reading the signalproduced by the reaction mixture stream; and (8) means for maintaining apressure of from 2-10 psi throughout the means comprising the FIAapparatus, whereby the sample, reagent composition, and reagent mixturestreams are individually and collectively impelled through said means,eventually to waste.
 2. An apparatus according to claim 1 wherein thefilter means is a tangential flow bypass membrane filter system; theheating means is an immersion heater; the first and second conduit meansare made of polyetheretherketone (PEEK) tubing; and the FIA apparatusadditionally includes computer means which process the data from thecolorimeter means together with other data which results in calculationof the concentration of total inorganic phosphate contained in theaqueous system from which the sample for testing was obtained.
 3. Anapparatus for flow injection analysis (FIA) determination by themolybdenum blue complex colorimetric reaction of total inorganicphosphate concentration in an aqueous system containing dissolvedinorganic polyphosphates as well as orthophosphate, comprising (1)filter means, selector valve means, and injection valve means forestablishing a filtered, continuously flowing sample stream from saidaqueous system to waste, from which sample units may be selected atdesignated intervals for passage through the FIA apparatus, by switchingof the injection valve means; (2) said injection valve means recitedabove, and separate mixing connector means which are connected andoperate together so as to have two switchable modes of operation: (a)when a sample unit is not to be analyzed, two reagent compositionstreams comprising a color-forming reagent and a reducing agent, arebrought together and admixed on a continuous basis at and by the mixingconnector means, the color-forming reagent flowing directly into saidmixing connector means, and the reducing agent flowing into said mixingconnector means after first passing through said injection valve means;and (b) when a sample unit is to be analyzed, the stream of reducingagent is interrupted by switching of said injection valve means recitedabove and the filtered sample stream is substituted therefor forsufficient time to select a sample unit, which then becomes admixed, atsaid mixing connector means, with the color-forming reagent stream,while bounded in front and behind by said reducing agent stream when theflow of the reducing agent stream is restored by switching of saidinjection valve means, thereby forming a reaction mixture of the sampleunit, color-forming reagent and reducing agent; (3) a first conduitmeans having two branches for separately connecting and carrying thesample stream and the reducing agent stream to said injection valvemeans, and from there a single branch to said mixing connector means;and a second conduit means for directly connecting and carrying thecolor-forming reagent stream to said mixing connector means withoutpassing through said injection valve means; (4) container means for thetwo reagent compositions, connected to the injection valve means and themixing connector means by said first and second conduit means as set outabove; (5) a third conduit means from the mixing connector means andeventually to waste, for carrying the reaction mixture stream formed bymixing of the sample stream and the two reagent composition streamsduring and subsequent to passage through said mixing connector means,said third conduit means being of sufficient length to permit completionof the colorimetric reaction in the reaction mixture stream; (6) heatingmeans through which the third conduit means passes for heating of thereaction mixture stream; (7) colorimetric means through which the thirdconduit means passes, having a 600-850 nm filter for reading the signalproduced by the reaction mixture stream; and (8) means for maintaining apressure of from 2-10 psi throughout the means comprising the FIAapparatus, whereby the sample, reagent composition, and reaction mixturestreams are individually and collectively impelled through said means,eventually to waste.
 4. An apparatus according to claim 3 wherein thefilter means is a targeted flow bypass membrane filter system; theheating means is an immersion heater; the first, second and thirdconduit means are made of polyetheretherketone (PEEK) tubing; the mixingconnector means is a T-connector; and the FIA apparatus additionallyincludes computer means which process the data from the colorimetermeans together with other known data which results in calculation of theconcentration of the total inorganic phosphate contained in the aqueoussystem from which the sample for testing was obtained.